FI773286A - PYRIMIDO (6,1-A) Isoquinolin-2-ON DERIVATIVES - Google Patents

PYRIMIDO (6,1-A) Isoquinolin-2-ON DERIVATIVES

Info

Publication number
FI773286A
FI773286A FI773286A FI773286A FI773286A FI 773286 A FI773286 A FI 773286A FI 773286 A FI773286 A FI 773286A FI 773286 A FI773286 A FI 773286A FI 773286 A FI773286 A FI 773286A
Authority
FI
Finland
Prior art keywords
alkyl
substd
opt
isoquinolin
pyrimido
Prior art date
Application number
FI773286A
Other languages
Finnish (fi)
Other versions
FI64370B (en
FI64370C (en
Inventor
Bansi Lal
Horst Dornauer
Bani Kanta Bhattacharya
Alihussein Nomanbha Dohadwalla
Noel John De Souza
Original Assignee
Hoechst Ag
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from DE19772720085 external-priority patent/DE2720085A1/en
Application filed by Hoechst Ag filed Critical Hoechst Ag
Publication of FI773286A publication Critical patent/FI773286A/en
Priority to FI813881A priority Critical patent/FI65778C/en
Publication of FI64370B publication Critical patent/FI64370B/en
Application granted granted Critical
Publication of FI64370C publication Critical patent/FI64370C/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/08Bronchodilators
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/08Antiallergic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/12Antihypertensives
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D217/00Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
    • C07D217/12Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with radicals, substituted by hetero atoms, attached to carbon atoms of the nitrogen-containing ring
    • C07D217/14Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with radicals, substituted by hetero atoms, attached to carbon atoms of the nitrogen-containing ring other than aralkyl radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/12Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains three hetero rings
    • C07D491/14Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/547Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/645Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having two nitrogen atoms as the only ring hetero atoms
    • C07F9/6509Six-membered rings
    • C07F9/650905Six-membered rings having the nitrogen atoms in the positions 1 and 2
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/547Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/6561Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing systems of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring or ring system, with or without other non-condensed hetero rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Molecular Biology (AREA)
  • Biochemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pulmonology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Cardiology (AREA)
  • Immunology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

Pyrimido 6,1-a isoquinolin-2-one derivs. of formula (I) and their acid-addn. and quat. ammonium salts are new: (where R1,R4 and R5 are H, OH, lower alkoxy, dialkyl-phosphinylalkoxy, acyloxy or halogen, or 2 adjacent group can form methyleneidoxy or ethylenedioxy; R2 and R3 are H, OH, lower alkoxy, NH2, alkylamino, dialkylamino, arylamino, alkyl, an amino or alkyl group substd. by a 5- or 6-membered ring contg. - 3 heteroatoms (N,S,S), cycloalkyl, hydroxyalkyl, alkoxyaylkyl, dialkoxyalkyl, haloalkyl, dialkylaminoalkyl, aralkyl, acyl or opt. substd. 6-10C aryl, or R2 is a pair of electrons if R6 is one of the radicals indicated below, or NR2R3 is an opt. substd. heterocycle opt. contg. another heteroatom (N or O); R6 is H, alkyl, cycloalkyl, hydorxyalkyl, alkoxyalkyl, dialkoxyalkyl, haloalkyl, alkyl-aminoalkhyl, aralkyl, heterocyclylalkyl, dialkylphosphinyl-alkyl, acyl or opt. substd. aryl, or R6 is a pair of electrons when R2 is one of the radicals indicated above). - (I) are useful as hypotensives, bronchodilators and allergic agents. A typical cpd. is 9,10-dimethoxy-4-t-butylamino-6,7-dihydro-2H-pyrim ido 6,1-alpha -isoquinolin-2-one. In an example, this is prepd. from 9,10-di-methoxy-4-chloro-6,7-dihydro-2H-pyrimido 6,1-1 -isoquinolin-2-one and t-butylamine.
FI773286A 1977-05-05 1977-11-02 PROCEDURE FOR THE FRAMEWORK OF THERAPEUTIC ANALYZA PYIMIDO- (6,1-A) Isoquinoline-2-IMINO-4-ONDERIVAT FI64370C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
FI813881A FI65778C (en) 1977-05-05 1981-12-03 PROCEDURE FOR THE PREPARATION OF THERAPEUTIC ANALYSIS OF PYIMIDO (6,1-A) Isoquinoline-2-AMINO-4-ONDERIVAT

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19772720085 DE2720085A1 (en) 1977-05-05 1977-05-05 PYRIMIDO (6.1-A) ISOCHINOLIN-2-ON DERIVATIVES
DE2720085 1977-05-05

Publications (3)

Publication Number Publication Date
FI773286A true FI773286A (en) 1978-11-06
FI64370B FI64370B (en) 1983-07-29
FI64370C FI64370C (en) 1983-11-10

Family

ID=6008073

Family Applications (1)

Application Number Title Priority Date Filing Date
FI773286A FI64370C (en) 1977-05-05 1977-11-02 PROCEDURE FOR THE FRAMEWORK OF THERAPEUTIC ANALYZA PYIMIDO- (6,1-A) Isoquinoline-2-IMINO-4-ONDERIVAT

Country Status (18)

Country Link
US (2) US4482556A (en)
JP (2) JPS53137997A (en)
AT (1) AT372383B (en)
BE (1) BE862785A (en)
CH (2) CH640854A5 (en)
DK (2) DK158789C (en)
EG (1) EG12982A (en)
ES (3) ES464776A1 (en)
FI (1) FI64370C (en)
FR (1) FR2389623B1 (en)
GR (1) GR72114B (en)
IL (1) IL53336A (en)
IT (1) IT1192252B (en)
NL (1) NL185078C (en)
NO (2) NO148032C (en)
PT (1) PT67265B (en)
SE (2) SE436357B (en)
ZA (1) ZA776706B (en)

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2847693A1 (en) * 1978-11-03 1980-05-22 Hoechst Ag METHOD FOR PRODUCING PYRIMIDO- (6,1-A) -ISOCHINOLIN-2-ONES
FR2470130A2 (en) * 1979-11-21 1981-05-29 Hoechst Ag Amino-pyrimido-isoquinolinone derivs. - useful as hypotensives, bronchodilators and antiallergic agents
DE3135831A1 (en) * 1981-09-10 1983-04-28 Hoechst Ag, 6230 Frankfurt 9,10-SUBSTITUTED 2-MESITYLIMINO-3-ALKYL-3,4,6,7-TETRAHYDRO-2H-PYRIMIDO (6.1-A) ISOCHINOLIN-4-ONE, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE AS A MEDICINAL PRODUCT
CA1237429A (en) * 1983-05-05 1988-05-31 Frank Kienzle Pyrimidone derivatives
DE3816995A1 (en) * 1988-05-19 1989-11-23 Hoechst Ag USE OF PYRIMIDO- (6,1-A) -ISOCHINOLIN-4-ON-DERIVATIVES AND MEDICAL PREPARATIONS BASED ON THESE COMPOUNDS
DE68902811D1 (en) * 1988-11-19 1992-10-15 Hoechst Ag PHARMACEUTICAL COMPOSITIONS CONTAINING LABDAN-DI-TERPENOID DERIVATIVES AND PYRIMIDO (6,1-A) ISOCHINOLIN-4-ON DERIVATIVES AND THEIR USE.
EP1165558B1 (en) * 1999-03-31 2003-09-24 Vernalis Limited Derivatives of pyrimido[6,1-a]isoquinolin-4-one
WO2005007092A2 (en) * 2003-07-08 2005-01-27 Smithkline Beecham Corporation Novel chemical compounds
CN101671336B (en) 2009-09-23 2013-11-13 辽宁利锋科技开发有限公司 Aromatic heterocyclic pyridine derivatives and analogs and preparation method and application thereof
GB201613054D0 (en) 2016-07-28 2016-09-14 Verona Pharma Plc New compound and process
IL280075B2 (en) * 2018-07-13 2024-06-01 Chia Tai Tianqing Pharmaceutical Group Co Ltd Fused tri-cyclic compound as pde3/pde4 dual inhibitor
EP4092025A4 (en) * 2020-01-15 2023-08-30 Chia Tai Tianqing Pharmaceutical Group Co., Ltd. Pharmaceutical composition of tricyclic pde3/pde4 dual inhibitor compound
WO2021143843A1 (en) * 2020-01-15 2021-07-22 正大天晴药业集团股份有限公司 Crystal of pde3/pde4 dual inhibitor and use thereof
WO2022228544A1 (en) * 2021-04-29 2022-11-03 苏州盛迪亚生物医药有限公司 Isoquinolone compound and use thereof
WO2024088402A1 (en) * 2022-10-28 2024-05-02 江苏恒瑞医药股份有限公司 Crystal form of isoquinolinone compound and preparation method therefor

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3021331A (en) * 1959-07-20 1962-02-13 Pfizer & Co C Azabenzopyridocolines
US3081306A (en) * 1959-11-04 1963-03-12 Pfizer & Co C 2, 4-dioxo-3-aralkylaza-9, 10-di(lower alkoxy)-1, 2, 3, 4, 6, 7-hexahydro-11b-h-benzopyridocolines
US3297696A (en) * 1965-05-28 1967-01-10 Sandoz Ag 6-amino-8, 9-dihydro-13bh-isoquinolo-[2, 1-c] quinazolines and intermediates therefor
DE2126148A1 (en) * 1971-05-26 1972-12-07 Farbenfabriken Bayer Ag, 5090 Leverkusen Prepn of uracil derivs - useful as plant - protection agents and their inters
DE2847693A1 (en) * 1978-11-03 1980-05-22 Hoechst Ag METHOD FOR PRODUCING PYRIMIDO- (6,1-A) -ISOCHINOLIN-2-ONES
US5740368A (en) * 1995-06-30 1998-04-14 Canon Kabushiki Kaisha Method and apparatus for providing information on a managed peripheral device to plural agents

Also Published As

Publication number Publication date
NL185078C (en) 1990-01-16
FR2389623B1 (en) 1980-10-31
CH642949A5 (en) 1984-05-15
FI64370B (en) 1983-07-29
CH640854A5 (en) 1984-01-31
DK267089A (en) 1989-06-01
DK158789C (en) 1990-11-26
NO148032C (en) 1983-07-27
FI64370C (en) 1983-11-10
SE8206619L (en) 1982-11-19
US4482556A (en) 1984-11-13
NO148032B (en) 1983-04-18
ZA776706B (en) 1978-08-30
IL53336A (en) 1984-02-29
GR72114B (en) 1983-09-15
SE436357B (en) 1984-12-03
DK267089D0 (en) 1989-06-01
PT67265B (en) 1981-01-05
ES475027A1 (en) 1979-05-16
EG12982A (en) 1982-03-31
ES472606A1 (en) 1979-02-16
NO821266L (en) 1978-11-07
AT372383B (en) 1983-09-26
SE439307B (en) 1985-06-10
IL53336A0 (en) 1978-01-31
US4598148A (en) 1986-07-01
ATA784477A (en) 1983-02-15
ES464776A1 (en) 1979-01-01
NL185078B (en) 1989-08-16
NL7800149A (en) 1978-11-07
NO774131L (en) 1978-11-07
IT1192252B (en) 1988-03-31
IT7822619A0 (en) 1978-04-21
JPS6312871B2 (en) 1988-03-23
DK489477A (en) 1978-11-06
JPS53137997A (en) 1978-12-01
SE7712513L (en) 1978-11-06
DK158789B (en) 1990-07-16
SE8206619D0 (en) 1982-11-19
JPS6041677A (en) 1985-03-05
JPS6225150B2 (en) 1987-06-01
BE862785A (en) 1978-07-10
PT67265A (en) 1977-12-01
FR2389623A1 (en) 1978-12-01

Similar Documents

Publication Publication Date Title
FI773286A (en) PYRIMIDO (6,1-A) Isoquinolin-2-ON DERIVATIVES
YU47195B (en) PROCEDURE FOR OBTAINING IMIDASOL DERIVATIVES AS CALCIUM OF INDEPENDENT PHOSPHODIESTERASE CAMP INHIBITORS
DE3486382D1 (en) Carboxyl-thio-pyrrolidinyl beta-lactam derivatives and their preparation.
ES2055705T3 (en) FUNGICIDES.
DK0649418T3 (en) 7- (2-amino ethyl) benzothiazolone
SE7606440L (en) NEW N-SUBSTITUTED BENZENESULPHONAMIDES AND METHODS OF PREPARING THE SAME
FR2581063B1 (en) AMINO-2 THIAZOLES N-SUBSTITUTED, THEIR PREPARATION PROCESS AND THEIR APPLICATION IN THERAPEUTICS
SE8201654L (en) Amido-AMINO ACIDS
ES2001697A6 (en) 2-Amino purines substituted in positions 6 and 9, their use, medicaments containing these purines and processes for their preparation.
ES457805A1 (en) Thiourea derivatives
SE7606424L (en) SUBSTITUTED BENZAMIDS
ES8602611A1 (en) Use of benzoylalanines as corrosion inhibitors in aqueous systems.
HUP9902149A2 (en) 1-methylcarbapenem derivatives with antibacterial activity, use thereof, pharmaceutical compositions containing these compounds
JPS56169614A (en) Hair cosmetic
IE41509L (en) Process for di- and triamino naphthalene production
ES480560A1 (en) Bridged catharanthus alkaloid dimers, their preparation and formulations containing them.
GB1463582A (en) Pyridine derivatives
DK272482A (en) TRICYCLIC RELATIONS
ES8308538A1 (en) Trifluoromethanesulfonanilides, and their production and use.
SU429582A3 (en) METHOD FOR OBTAINING 2,6-5H-(DIALKANOLAMINO)PYRIMIDO[5,4-c{] PYRIMIDINE1 DERIVATIVES ?] pyrimidine described in the literature have the best pharmacological properties. A method is known for obtaining pyrimido[5,4-th]-pyrimidines of the general formula by reducing the compound of general formula-1 B10, where two of the radicals Ri, R2, Rs and R4 are a free or substituted amino group or a free or substituted hydrazino or guanidino group, and the other two are hydrogen or halogen, an alkyl or aryl radical, an hydroxy group free or substituted by an alkyl, Ery;!-yl'I diethylamioethyl group, a mercapto group, free or substituted by an alkyl or an aryl radical. npa and one more of the Zi, Z^, Zg and Z4 radicals is hydrogen or halogen, alkyl or aryl, an hydroxy group free or substituted by an alkyl, aryl or diethylaminoethyl group, a mercapto group free or substituted by an alkyl or aryl radical, or a free or substituted amino group. We propose a method.
DE3864428D1 (en) HAIR DYE WITH DIRECT DRAWING NITRODIPHENYLAMINE DERIVATIVES.
GB1008454A (en) Pseudoxanthines
FR2035768A1 (en) Pyrimidine-based medicament having local - anaesthetic antitussive and antiinflammatory
FR2393001A1 (en) Antiinflammatory and sedative thiazolo quinazoline cpds. - prepd. from anthranilic ester and isothiocyanato di:ethylamino butyne
FR2256761A1 (en) 2,4-Benzothiazepine condensed ring derivs - prepd. by cyclizing e.g. 2-halomethyl-benzhydryl heterocyclyl thioethers

Legal Events

Date Code Title Description
MM Patent lapsed

Owner name: HOECHST AG